A tight-binding dimer model shows that the laser polarization maximizing high-harmonic yield flips from molecular axes to the intermolecular axis at higher orders, with the flip order depending on coupling strength, and this behavior is already present in adiabatically following states.
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Isolated attosecond pulses recover photoelectron spectral phase from spectra, allowing time-resolved mapping of electron birth in circularly polarized strong-field ionization.
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High-harmonic generation from two weakly coupled molecules: a simple tight-binding model
A tight-binding dimer model shows that the laser polarization maximizing high-harmonic yield flips from molecular axes to the intermolecular axis at higher orders, with the flip order depending on coupling strength, and this behavior is already present in adiabatically following states.
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Time-resolving the birth of photoelectrons in strong-filed ionization with an isolated attosecond pulse
Isolated attosecond pulses recover photoelectron spectral phase from spectra, allowing time-resolved mapping of electron birth in circularly polarized strong-field ionization.